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共添加策略增强烟曲霉 CY018 深层发酵中白僵菌素。

Co-addition Strategy for Enhancement of Chaetominine from Submerged Fermentation of Aspergillus fumigatus CY018.

机构信息

State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Box 283#, 130 Meilong Road, Shanghai, 200237, People's Republic of China.

出版信息

Appl Biochem Biotechnol. 2018 Oct;186(2):384-399. doi: 10.1007/s12010-018-2714-6. Epub 2018 Apr 10.

Abstract

Chaetominine (CHA), a novel framework tripeptide alkaloid, imparts an attractive cytotoxic against the human leukemia cell line K562, which is produced by Aspergillus fumigatus CY018. However, its pharmacological research is restricted by low yields in submerged culture, which needs to be resolved immediately by biotechnology. In this work, a co-addition strategy was applied to promote CHA production based on related inhibitors' addition and precursors' addition, inspired by the biosynthetic pathway analysis of CHA. CHA production reached 53.87 mg/L by addition of 10 mM shikimate, 10 mM anthranilate, 20 mM tryptophan, and 10 mM alanine in shake flask. Compared to the control without addition of precursors, the activity of 3-deoxy-arabino-heptulosonate-7-phospahte (DAHP) synthase was significantly improved and the transcription levels of critical genes in shikimate pathway were up-regulated responded to the co-addition of precursors. The improvement of CHA production by co-addition of precursors was also successfully reproduced in the lab-scale bioreactor (5-L) system, in which CHA production reached 46.10 mg/L. This work demonstrated that precursors' co-addition was an effective strategy for increasing CHA production, and the information obtained might be useful to the further improvement of CHA on a large scale.

摘要

麦角硫因(CHA)是一种新型骨架三肽生物碱,对人白血病细胞系 K562 具有很强的细胞毒性,该化合物由烟曲霉 CY018 产生。然而,由于其在液体深层发酵中产量较低,限制了其药理学研究,需要立即通过生物技术加以解决。在这项工作中,基于 CHA 的生物合成途径分析,应用共添加策略来促进 CHA 的产生,包括添加相关抑制剂和前体。通过在摇瓶中添加 10 mM 莽草酸、10 mM 邻氨基苯甲酸、20 mM 色氨酸和 10 mM 丙氨酸,CHA 的产量达到 53.87mg/L。与不添加前体的对照相比,3-脱氧阿拉伯庚酮糖-7-磷酸(DAHP)合酶的活性显著提高,莽草酸途径中关键基因的转录水平也相应上调,对前体共添加有响应。在实验室规模的生物反应器(5-L)系统中,共添加前体也成功地再现了 CHA 产量的提高,在该系统中,CHA 的产量达到 46.10mg/L。这项工作表明,前体共添加是提高 CHA 产量的有效策略,获得的信息可能对进一步提高 CHA 的产量具有重要意义。

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